CC BY-NC-ND 4.0 · European Journal of General Dentistry 2014; 3(01): 22-28
DOI: 10.4103/2278-9626.126205
Original Article

Insights into functional tea infused-chitosan hydrogels as potential bio-active restorative materials

Tamara V. Perchyonok
School of Dentistry and Oral Health, Research and Development, VTPCHEM PTY LTD, Griffith University, Southport QLD 4215, Melbourne, Victoria 3163, Australia
,
Shengmiao Zhang
1   School of Material Science and Engineering, East China University of Science and Technology, Shanghai 200237, China
,
Sias Grobler
2   Faculty of Dentistry, Oral and Dental Research Institute, University of the Western Cape, Private Bag X1, Tygerberg 7505, Cape Town, South Africa
,
Theunis Oberholzer
School of Dentistry and Oral Health, Research and Development, VTPCHEM PTY LTD, Griffith University, Southport QLD 4215, Melbourne, Victoria 3163, Australia
,
Ward Massey
School of Dentistry and Oral Health, Research and Development, VTPCHEM PTY LTD, Griffith University, Southport QLD 4215, Melbourne, Victoria 3163, Australia
› Author Affiliations

Abstract

Introduction: We described novel chitosan hydrogels (chitosan-H) containing tea infusions (green, red and black) as functional additive prototypes with special focus on the design and functionality of dual action composite restorative materials. Their intended uses include remineralizing bases/liners, therapeutically active restorative materials and/or functional additives as well as functional prototype of the drug delivery system. Materials and Methods: The above mentioned hydrogels were prepared by dispersion of the corresponding component in glycerol and acetic acid with the addition of chitosan gelling agent. The surface morphology scanning electron microscope (SEM), release behavior (physiological pH as well as acidic conditions), stability of the hydrogels as well as antioxidant capacity of the tea infused hydrogels was evaluated. Results: It was found that all the anti-oxidant chitosan-H hydrogels treated dentine gave significantly (P < 0.05; Non-parametric ANOVA test) higher shear bond strength values than dentine treated or not treated with phosphoric acid. Overall, there was a small relapse in the shear bond strength after 6 months. The SEM is employed to observe the surface of the newly made functional restorative materials. The anti-oxidant capacity of various black, red and green tea infusions was investigated and demonstrated increased antioxidant stability of the newly prepared material stability. Conclusion: We have developed and evaluated several functional chitosan hydrogels with several targets as therapeutic restorative materials, the added benefits of their unique functionality involve increased dentin adhesive bond strengths (after 24 h and after 6 month), concept of using functional materials as carriers for pro-drugs as well as display certain degree of defense mechanism for a free radical damage.



Publication History

Article published online:
01 November 2021

© 2014. European Journal of General Dentistry. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/.)

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  • References

  • 1 Ratner BD, Hoffman D, Schoen FJ, Lemons JE. Biomaterial Science: An Introduction to Materials in Medicine. San Diego: Academic Press; 2004.
  • 2 Shi D. Biomaterials and Tissue Engineering. Berlin, Heidelberg: Springer-Verlag; 2004.
  • 3 Menaa B, Menaa F, Aiolfi-Guimaraes C, Sharts O. Silica-based nanoporous sol-gel glasses: From bioencapsulation to protein folding studies. Int J Nanotechnol 2010;7:1-45.
  • 4 Anand SC, Kennedy JF, Miraftab M, Rajendran S. Medical Textiles and Biomaterials for Healthcare. Cambridge: Woodhead Publishing Ltd.; 2006.
  • 5 Park JH, Saravanakumar G, Kim K, Kwon IC. Targeted delivery of low molecular drugs using chitosan and its derivatives. Adv Drug Deliv Rev 2010;62:28-41.
  • 6 Balcerzak J, Mucha M. Analysis of model drug release kinetics from complex matrices of polylactice-chitosan. Progress on Chemistry and Application of Chitin and its Derivatives. 2010. p. 15117-25.
  • 7 Perchyonok T, Zhang S, Oberholzer T. Protective effect of conventional antioxidant (beta-carotene, resveratrol and vitamin e) in chitosan-containing hydrogels against oxidative stress and reversal of DNA double stranded breaks induced by common dental composites: In-vitro model. Open Nanosci J 2013;71:1-7.
  • 8 Perchyonok T, Lykakis I, Postigo A. Streamlining Free Radical Green Chemistry. Cambridge: The Royal Society of Chemistry; 2012.
  • 9 Perchyonok T, Zhang S, Oberholzer TG. Alternative chitosan based drug delivery system to fight oral mucositis: Synergy of conventional and bioactives towards the optimal solution. Curr Nanosci 2012;8:541-7.
  • 10 Perchyonok VT, Zhang S, Oberholzer T. Chitosan and gelatin based prototype delivery systems for the treatment of oral mucositis: From material to performance in vitro. Curr Drug Deliv 2013;10:144-50.
  • 11 Jin D, Hakamata H, Takahashi K, Kotani A, Kusu F. Determination of quercetin in human plasma after ingestion of commercial canned green tea by semi-micro HPLC with electrochemical detection. Biomed Chromatogr 2004;18:662-6.
  • 12 Pelillo M, Bonoli M, Biguzzi B, Bendini A, Toschi TG, Lercker G. An investigation in the use of HPLC with UV and MS electrospray detection for the quantification of tea catechins. Food Chem 2004;87:465-70.
  • 13 Karakaya S, Kavas A. Antimutagenic activities of some foods. J Sci Food Agric 1999;79:237-42.
  • 14 Re R, Pellegrini N, Proteggente A, Pannala A, Yang M, Rice-Evans C. Antioxidant activity applying an improved ABTS radical cation decolorization assay. Free Radic Biol Med 1999;26:1231-7.
  • 15 Peak MJ, Peak JG. Hydroxyl radical quenching agents protect against DNA breakage caused by both 365-nm UVA and by gamma radiation. Photochem Photobiol 1990;51:649-52.
  • 16 Bartold PM, Wiebkin OW, Thonard JC. The effect of oxygen-derived free radicals on gingival proteoglycans and hyaluronic acid. J Periodontal Res 1984;19:390-400.
  • 17 Chapple IL. Role of free radicals and antioxidants in the pathogenesis of the inflammatory periodontal diseases. Clin Mol Pathol 1996;49:M247-55.
  • 18 Nagy I, Floyd RA. Electron spin resonance spectroscopic demonstration of the hydroxyl free radical scavenger properties of dimethylaminoethanol in spin trapping experiments confirming the molecular basis for the biological effects of centrophenoxine. Arch Gerontol Geriatr 1984;3:297-310.
  • 19 Zs -Nagy I, Floyd RA. ESR spin trapping studies on the OHFNx01 free radical reactions of idebenone. Arch Gerontol Geriatr 1990;11:215-31.
  • 20 Godley BF, Shamsi FA, Liang FQ, Jarrett SG, Davies S, Boulton M. Epithelial cells damage and free radical production in blue light induces mitochondrial DNA. The Journal of Biological Chemistry, 280:21061-6.
  • 21 Chattopadhyay P, Besra SE, Gomes A, Das M, Sur P, Mitra S, et al. Anti-inflammatory activity of tea (Camellia sinensis) root extract. Life Sci 2004;74:1839-49.